JPH0617320B2 - イソブテンを製造する方法 - Google Patents

イソブテンを製造する方法

Info

Publication number: JPH0617320B2
Authority: JP; Japan
Prior art keywords: propylene; isobutene; feed; bar; weight
Prior art date: 1984-04-03
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Expired - Lifetime

Application number

JP60069249A

Other languages

English (en)

Japanese (ja)

Other versions

JPS60224639A (ja

Inventor

ガイ・エル・ジー・デブラス

ジヨルジユ・イー・エム・ジエイ・ド・クリツプレ

レイモンド・エム・カヘン

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Labofina SA

Original Assignee

Labofina SA

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1984-04-03

Filing date

1985-04-03

Publication date

1994-03-09

1985-04-03 Application filed by Labofina SA filed Critical Labofina SA

1985-11-09 Publication of JPS60224639A publication Critical patent/JPS60224639A/ja

1994-03-09 Publication of JPH0617320B2 publication Critical patent/JPH0617320B2/ja

2009-03-09 Anticipated expiration legal-status Critical

Status Expired - Lifetime legal-status Critical Current

Links

VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical compound CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 title claims description 82
238000004519 manufacturing process Methods 0.000 title claims description 13
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 44
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 42
238000000034 method Methods 0.000 claims description 32
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 26
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 19
230000008569 process Effects 0.000 claims description 17
239000003054 catalyst Substances 0.000 claims description 11
235000012239 silicon dioxide Nutrition 0.000 claims description 5
229910002026 crystalline silica Inorganic materials 0.000 claims description 4
239000011541 reaction mixture Substances 0.000 claims description 3
ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 20
238000006243 chemical reaction Methods 0.000 description 14
239000007789 gas Substances 0.000 description 13
239000001294 propane Substances 0.000 description 10
239000000203 mixture Substances 0.000 description 9
BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 description 4
239000007795 chemical reaction product Substances 0.000 description 4
229930195733 hydrocarbon Natural products 0.000 description 4
150000002430 hydrocarbons Chemical class 0.000 description 4
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
239000000654 additive Substances 0.000 description 3
150000001336 alkenes Chemical class 0.000 description 3
238000004523 catalytic cracking Methods 0.000 description 3
239000000446 fuel Substances 0.000 description 3
239000000047 product Substances 0.000 description 3
239000007858 starting material Substances 0.000 description 3
DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
238000009835 boiling Methods 0.000 description 2
238000004231 fluid catalytic cracking Methods 0.000 description 2
239000007788 liquid Substances 0.000 description 2
238000012986 modification Methods 0.000 description 2
230000004048 modification Effects 0.000 description 2
239000003921 oil Substances 0.000 description 2
238000006384 oligomerization reaction Methods 0.000 description 2
239000000377 silicon dioxide Substances 0.000 description 2
MRMOZBOQVYRSEM-UHFFFAOYSA-N tetraethyllead Chemical compound CC[Pb](CC)(CC)CC MRMOZBOQVYRSEM-UHFFFAOYSA-N 0.000 description 2
VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 1
WJQOZHYUIDYNHM-UHFFFAOYSA-N 2-tert-Butylphenol Chemical compound CC(C)(C)C1=CC=CC=C1O WJQOZHYUIDYNHM-UHFFFAOYSA-N 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
239000001273 butane Substances 0.000 description 1
IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 1
125000004432 carbon atom Chemical group C* 0.000 description 1
230000015556 catabolic process Effects 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
150000001875 compounds Chemical class 0.000 description 1
238000005336 cracking Methods 0.000 description 1
238000006731 degradation reaction Methods 0.000 description 1
238000004821 distillation Methods 0.000 description 1
238000009826 distribution Methods 0.000 description 1
230000002708 enhancing effect Effects 0.000 description 1
230000007613 environmental effect Effects 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
239000003254 gasoline additive Substances 0.000 description 1
238000005984 hydrogenation reaction Methods 0.000 description 1
239000012535 impurity Substances 0.000 description 1
239000007791 liquid phase Substances 0.000 description 1
239000010687 lubricating oil Substances 0.000 description 1
239000002808 molecular sieve Substances 0.000 description 1
IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
230000003606 oligomerizing effect Effects 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
239000012071 phase Substances 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
239000011148 porous material Substances 0.000 description 1
238000011084 recovery Methods 0.000 description 1
238000007670 refining Methods 0.000 description 1
238000011160 research Methods 0.000 description 1
229930195734 saturated hydrocarbon Natural products 0.000 description 1
URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 1
239000002904 solvent Substances 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
239000000126 substance Substances 0.000 description 1
238000012360 testing method Methods 0.000 description 1
125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
239000002912 waste gas Substances 0.000 description 1
239000002699 waste material Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C6/00—Preparation of hydrocarbons from hydrocarbons containing a different number of carbon atoms by redistribution reactions
- C07C6/02—Metathesis reactions at an unsaturated carbon-to-carbon bond
- C07C6/04—Metathesis reactions at an unsaturated carbon-to-carbon bond at a carbon-to-carbon double bond

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Catalysts (AREA)
Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

JP60069249A 1984-04-03 1985-04-03 イソブテンを製造する方法 Expired - Lifetime JPH0617320B2 (ja)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
LU85284		1984-04-03
LU85284A LU85284A1 (fr)	1984-04-03	1984-04-03	Procede de production d'isobutylene

Publications (2)

Publication Number	Publication Date
JPS60224639A JPS60224639A (ja)	1985-11-09
JPH0617320B2 true JPH0617320B2 (ja)	1994-03-09

Family

ID=19730234

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP60069249A Expired - Lifetime JPH0617320B2 (ja)	1984-04-03	1985-04-03	イソブテンを製造する方法

Country Status (10)

Country	Link
US (1)	US4556753A (fr)
JP (1)	JPH0617320B2 (fr)
BE (1)	BE902090A (fr)
CA (1)	CA1238654A (fr)
DE (1)	DE3510764C2 (fr)
FR (1)	FR2562066B1 (fr)
GB (1)	GB2156845B (fr)
IT (1)	IT1183535B (fr)
LU (1)	LU85284A1 (fr)
NL (1)	NL193866C (fr)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
LU85406A1 (fr) *	1984-06-06	1986-01-24	Labofina Sa	Procede de craquage catalytique de distillets legers
US5164071A (en) *	1989-04-17	1992-11-17	Mobil Oil Corporation	Fluidized catalyst process for upgrading olefins
EP0920911A1 (fr)	1997-12-05	1999-06-09	Fina Research S.A.	Production de catalyseurs pour la conversion d'oléfines

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3723562A (en) *	1970-10-08	1973-03-27	Phillips Petroleum Co	Conversion of olefins
US4423269A (en) *	1981-09-25	1983-12-27	Chevron Research Company	Oligomerization of gaseous olefins
US4511746A (en) *	1981-09-25	1985-04-16	Chevron Research Company	Low activity catalyst oligomerization process
US4579989A (en) *	1983-05-20	1986-04-01	Cosden Technology, Inc.	Conversion of olefins to higher molecular weight hydrocarbons with silicalite catalyst

1984
- 1984-04-03 LU LU85284A patent/LU85284A1/fr unknown
1985
- 1985-03-13 GB GB08506517A patent/GB2156845B/en not_active Expired
- 1985-03-15 FR FR8503817A patent/FR2562066B1/fr not_active Expired
- 1985-03-19 NL NL8500789A patent/NL193866C/nl not_active IP Right Cessation
- 1985-03-25 DE DE3510764A patent/DE3510764C2/de not_active Expired - Fee Related
- 1985-03-28 CA CA000477741A patent/CA1238654A/fr not_active Expired
- 1985-03-29 IT IT20166/85A patent/IT1183535B/it active
- 1985-04-02 BE BE0/214765A patent/BE902090A/fr not_active IP Right Cessation
- 1985-04-03 US US06/719,192 patent/US4556753A/en not_active Expired - Lifetime
- 1985-04-03 JP JP60069249A patent/JPH0617320B2/ja not_active Expired - Lifetime

Also Published As

Publication number	Publication date
IT1183535B (it)	1987-10-22
NL193866C (nl)	2001-01-03
GB2156845A (en)	1985-10-16
NL8500789A (nl)	1985-11-01
FR2562066B1 (fr)	1987-12-24
DE3510764C2 (de)	1994-02-03
FR2562066A1 (fr)	1985-10-04
NL193866B (nl)	2000-09-01
GB2156845B (en)	1987-10-14
DE3510764A1 (de)	1985-10-10
BE902090A (fr)	1985-10-02
GB8506517D0 (en)	1985-04-17
JPS60224639A (ja)	1985-11-09
CA1238654A (fr)	1988-06-28
US4556753A (en)	1985-12-03
IT8520166A0 (it)	1985-03-29
LU85284A1 (fr)	1985-11-27

Publication	Publication Date	Title
KR101759802B1 (ko)	2017-07-19	저 에틸렌 또는 에틸렌을 이용하지 않는 복분해를 통한 프로필렌
US4587375A (en)	1986-05-06	Process for the isomerization of olefins
Asinger	2013	Mono-olefins: chemistry and technology
KR20040095272A (ko)	2004-11-12	Ｃ4 올레핀 스트림으로부터 프로필렌과 헥센을 제조하는방법
US6872862B2 (en)	2005-03-29	Propylene production
US5698760A (en)	1997-12-16	Olefin metathesis
JPS6016939A (ja)	1985-01-28	Ｃ↓４留分の重合によるハイオクタンガソリンの製造法
GB2171718A (en)	1986-09-03	Olefin preparation
US4140621A (en)	1979-02-20	Maintaining or increasing the isobutane content of a cut subjected to selective hydrogenolysis
US6156947A (en)	2000-12-05	Process for the production of butene-1 from a mixture of C4 olefins
EP1178029A1 (fr)	2002-02-06	Procédé pour la préparation de di-isobutanes, de di-iosbutènes et de di-n-butènes à partir de butane naturel
US3751514A (en)	1973-08-07	Preparation of isobutylene and propylene from isobutane
US20040192994A1 (en)	2004-09-30	Propylene production
KR101524487B1 (ko)	2015-06-01	Ｃ5 탄화수소를 함유하는 스트림에 또한 함유된 이소부텐의 선택적 이합체화 반응에 의한 고-옥탄 탄화수소 화합물의 제조를 위한 공정
US5912191A (en)	1999-06-15	Process for preparing alkyl tert-butyl ethers and di-n-butene from field butanes
US4556753A (en)	1985-12-03	Process for producing isobutene
US2322122A (en)	1943-06-15	Method of preparing butadiene
CA1250004A (fr)	1989-02-14	Production d'isobutene
US5864052A (en)	1999-01-26	Process for preparing alkyl tert-butyl ethers and di-n-butene from field butanes
AU2003297339B2 (en)	2007-04-26	Process for separating linear alpha olefins from saturated hydrocarbons
US6884917B1 (en)	2005-04-26	1-butene production
AU636213B2 (en)	1993-04-22	Production of diisopropyl ether
KR20250034384A (ko)	2025-03-11	C4 탄화수소로부터 mtbe 및 말레산 무수물을 생산하기 위한 시스템 및 공정
Daubert et al.	1963	Conversion of Gas Oils by Oxidation.